Canonical Allele Identifier: CA244637595
Gene:

Linked Data

dbSNP Id: rs765303909
MyVariant Identifiers: chr12:g.115398645G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398645G>T , CM000674.2:g.115398645G>T GRCh38
NC_000012.11:g.115836450G>T , CM000674.1:g.115836450G>T GRCh37
NC_000012.10:g.114320833G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945389.1:n.697+8450C>A
XR_945389.2:n.701+8450C>A